SCHEMBL2945494

SCHEMBL2945494

CCC(C)CC(O)C(=O)O

nearest known ligand 0.46

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
OR51E2 Q9H255 1/20 0.42
GPR84 Q9NQS5 3/20 0.41
FFAR1 O14842 1/20 0.41
TP53 P04637 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.40
TET2 Q6N021 3/20 0.37
KDM4A O75164 2/20 0.37
KDM4C Q9H3R0 2/20 0.37
KDM2A Q9Y2K7 2/20 0.37
TET3 O43151 1/20 0.37
SLC1A3 P43003 1/20 0.37
SLC1A2 P43004 1/20 0.37
SLC1A1 P43005 1/20 0.37
ALDH1A1 P00352 1/20 0.36
TSHR P16473 1/20 0.36
RNPEP Q9H4A4 1/20 0.36
SLC7A5 Q01650 1/20 0.36
FOLH1 Q04609 1/20 0.35
NAALAD2 Q9Y3Q0 1/20 0.35

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL8495464 1.00 OR51E2 (0.42) OR51E2GPR84FFAR1TP53SMN1; SMN2
SCHEMBL14661739 1.00 OR51E2 (0.42) OR51E2GPR84FFAR1TP53SMN1; SMN2
SCHEMBL14661746 1.00 OR51E2 (0.42) OR51E2GPR84FFAR1TP53SMN1; SMN2
SCHEMBL14661330 1.00 OR51E2 (0.42) OR51E2GPR84FFAR1TP53SMN1; SMN2
SCHEMBL14662148 1.00 OR51E2 (0.42) OR51E2GPR84FFAR1TP53SMN1; SMN2
SCHEMBL28482603 0.87 OR51E2 (0.48) OR51E2GPR84FFAR1TP53SMN1; SMN2
SCHEMBL28492635 0.84 OR51E2 (0.46) OR51E2GPR84FFAR1TP53SMN1; SMN2
Ammonia Solution, Strong SCHEMBL28482605 0.84 OR51E2 (0.46) OR51E2GPR84FFAR1TP53SMN1; SMN2
SCHEMBL2231168 0.81 GPR84 (0.48) OR51E2GPR84FFAR1TP53SMN1; SMN2
SCHEMBL14661520 0.81 GPR84 (0.48) OR51E2GPR84FFAR1TP53SMN1; SMN2

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 30 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2009127009-A1 CONDENSATION POLYMERS COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANISATION (AU) 2009-10-22 WO claimed
EP-0000560-B1 PROCESS FOR THE PREPARATION OF OPTICALLY ACTIVE ALPHA-HYDROXYCARBOXYLIC ACIDS F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1982-02-03 EP claimed
US-4204044-A SELECTIVE ASYMMETRIC, ENZYMATIC DEHYDROGENATIKN USING STREPTOMYCES, PSEUDOMONAS, BACILLUS OR CORYNEFORM MICROORGANISMS HOFFMANN-LA ROCHE INC. (US) 1980-05-20 US claimed
EP-0000560-A1 Process for the preparation of optically active alpha-hydroxycarboxylic acids F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1979-02-07 EP claimed
US-20240397944-A1 METHODS FOR BIOFILM DISRUPTION Lixa Limited (AU) 2024-12-05 US disclosed
CN-115715547-B Nematode extract and application thereof 沈阳恩柽研究院有限公司 2024-11-29 CN disclosed
CN-115715547-A Nematode extract and application thereof 沈阳恩柽研究院有限公司 2023-02-28 CN disclosed
CN-113796390-B Nematode extract and application thereof 沈阳恩柽研究院有限公司 2022-12-13 CN disclosed
CN-113796390-A Nematode extract and application thereof 沈阳恩柽研究院有限公司 2021-12-17 CN disclosed
CN-105018384-B One plant of acetic acid bacteria and its application in the apple vinegar that ferments 江南大学 2018-07-06 CN disclosed
US-9688809-B2 Method for purifying aliphatic polyester and aliphatic polyester purified with said method MUSASHINO CHEMICAL LABORATORY, LTD. (JP) 2017-06-27 US disclosed
US-20160083507-A1 METHOD FOR PURIFYING ALIPHATIC POLYESTER AND ALIPHATIC POLYESTER PURIFIED WITH SAID METHOD MUSASHINO CHEMICAL LABORATORY, LTD. (JP) 2016-03-24 US disclosed
WO-2009031762-A2 RECOMBINANT MICROORGANISM CAPABLE OF PRODUCING POLYLACTATE OR POLYLACTATE COPOLYMER FROM SUCROSE AND METHOD FOR PRODUCING POLYLACTATE OR POLYLACTATE COPOLYMER FROM SUCROSE USING THE SAME LG CHEM, LTD. (KR) 2009-03-12 WO disclosed
EP-1961739-A1 NOVEL COMPOUND, POLYMER, AND RESIN COMPOSITION JSR Corporation (JP) 2008-08-27 EP disclosed
EP-1953595-A1 RADIATION-SENSITIVE RESIN COMPOSITION JSR Corporation (JP) 2008-08-06 EP disclosed
US-7235251-B2 Cosmetic or dermatological oil/water emulsions with reduced lipid content BEIERSDORF AG (DE) 2007-06-26 US disclosed
US-20030125386-A1 Fatty acid nutritional supplement BAYLOR UNIVERSITY MEDICAL CENTER 2003-07-03 US disclosed
EP-0000560-B1 PROCESS FOR THE PREPARATION OF OPTICALLY ACTIVE ALPHA-HYDROXYCARBOXYLIC ACIDS F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1982-02-03 EP disclosed
US-4204044-A SELECTIVE ASYMMETRIC, ENZYMATIC DEHYDROGENATIKN USING STREPTOMYCES, PSEUDOMONAS, BACILLUS OR CORYNEFORM MICROORGANISMS HOFFMANN-LA ROCHE INC. (US) 1980-05-20 US disclosed
EP-0000560-A1 Process for the preparation of optically active alpha-hydroxycarboxylic acids F. HOFFMANN-LA ROCHE & CO. Aktiengesellschaft (CH) 1979-02-07 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20240397944-A1 METHODS FOR BIOFILM DISRUPTION FGB, MMP8, HAO2 OR51E2 3431/4885GPR84 3312/4885FFAR1 1313/4885
US-20030125386-A1 Fatty acid nutritional supplement FASN, SLC27A1, SLC27A2 OR51E2 4176/4885GPR84 460/4885FFAR1 27/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.